Intermediates and improved processes for the preparation of neplanocin A

ABSTRACT

Intermediate compounds, including 2-(t-butyldimethylsilyloxymethyl)-3,4-[(dimethylmethylene)dioxy]-5-hydroxy-tricyclo[5.2.1.0 2,6 ]dec-8-ene, which are useful for the synthesis of neplanocin A having strong antitumor activity. Improved processes for the preparation of neplanocin A, starting from optically active 2-hydroxymethyl-5-hydroxy-tricyclo[5.2.1.0 2,6 ]deca-3,8-diene and via a key step comprising a retro-Diels-Alder reaction of the above intermediate.

RELATED APPLICATIONS

This application, concurrently filed with copending divisionalapplication Ser. No. 10/369,686, filed Feb. 18, 2003 Ser. No. 10/369,510filed Feb. 21, 2003 and Ser. No. 10/369,532, filed Feb. 21, 2003 is adivisional of application Ser. No. 09/849,356, filed May 7, 2001, nowU.S. Pat. No. 6,642,424, which is a divisional of application Ser. No.09/318,435, filed May 25, 1999, now U.S. Pat. No. 6,265,209.

This invention relates to compounds, including2-(t-butyldimethylsilyloxymethyl)-3,4-[(dimethylmethylene)-dioxy]-5-hydroxy-tricyclo[5.2.1.0^(2,6)]dec-8-eneand the analogues thereof, which are useful as intermediates for thesynthesis of neplanocin A having strong antitumor activity. Theinvention also relates to improved processes for the preparation ofneplanocin A.

BACKGROUND OF THE INVENTION

Neplanocin A is represented by the following formula and one ofcarbanucleosides having strong antitumor activity, but it is not itselfa sufficient drug for the clinical treatment of cancer, because of itsstrong adverse effect.

Nevertheless, there have been desired improved methods for efficientlypreparing neplanocin A and related compounds.

Vandewalle et al. (Synlett, December 1991, 921–922) disclose thesynthesis of (−)-neplanocin A starting from L-ribulose in 14 steps andin 15% overall yield. Ohira et al. (Tetrahedron Letters, vol. 36, No. 9,pp. 1537–1538, 1995) disclose the synthesis of (−)-neplanocin A startingfrom D-ribose modified with the protecting group in 9 steps and in 12%overall yield. Trost et al. (Tetrahedron Letters, vol. 38, No. 10, pp.1707–1710, 1997) disclose the stereoselective synthesis of(−)-neplanocin A using an asymmetric catalyst in 13 steps and in 4%overall yield. Thus, the above prior processes require more improvementin the process step and yield.

SUMMARY OF THE INVENTION

The present invention provides a group of intermediates useful for thesynthesis of neplanocin A and related compounds which improve ourflexibility in exploring structural variation of carbanucleosides havingpotential use including chemotherapeutic agents.

The invention also relates to improved processes for the preparation ofneplanocin A in short process step and in high yield, starting from acompound of the following formula (1) and via a compound of thefollowing formula (6).

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides new class of the compounds useful asintermediates for the synthesis of neplanocin A, which includes thecompounds of the following formulas:

-   Formula (1)

wherein R₁ and R₂ are independently hydrogen or an alkanoyl group of2–20 carbons;

-   Formula (2)

wherein X is halogen;

-   Formula (3)

wherein X is halogen and Y is a protecting group;

-   Formula (4)

wherein X is halogen and Y is a protecting group;

-   Formula (5)

wherein X is halogen and Y is a protecting group;

-   Formula (6)

wherein Y is a protecting group;

-   Formula (7)

wherein Y is a protecting group;

-   Formula (8)

wherein Y is a protecting group;

-   Formula (9)

wherein Y is a protecting group;

-   Formula (10)

wherein Y is a protecting group.

Examples of the alkanoyl group of 2–20 carbons for R₁ and R₂ include,but are not limited to, acetyl, propionyl, butyryl, isobutyryl, valeryl,isovaleryl, pivaloyl, lauroyl, myristoyl, palmitoyl, stearoyl, caproyl,enanthoyl, capryloyl and icosanoyl. Examples of the halogen for X areCl, Br and I.

The protecting groups for Y can include any group known in the art oforganic synthesis for the protection of hydroxyl groups. Examples ofsuch protecting group include, but are not limited, to trimethylsilyl,triethylsilyl, t-butyldimethylsilyl (TBS), t-butyldiphenylsilyl,methoxymethyl, methoxyethoxymethyl, t-butyl, benzyl, triphenylmethyl,isopropyldimethylsilyl, tribenzylsilyl and triisopropylsilyl.

Specific compounds within formulas (2)–(10) are represented by thefollowing respective formulas (2a)–(10a):

wherein TBS stands for t-butyldimethylsilyl.

The present invention also provides a process for the preparation ofneplanocin A which comprises the steps of:

-   (a) reacting a compound of formula (1′)

with a halogenating agent, to form a compound of formula (2)

wherein X is halogen;

-   (b) reacting the compound (2) with an agent for the protection of    hydroxyl groups, to form a compound of formula (3)

wherein X is as defined above and Y is a protecting group;

-   (c) treating the compound (3) with an oxidizing agent, to form a    compound of formula (4)

wherein X and Y are as defined above;

-   (d) reacting the compound (4) with a ketalizing agent, to form a    compound of formula (5)

wherein X and Y are as defined above;

-   (e) treating the compound (5) with a dehalogenating agent, to form a    compound of formula (6)

wherein Y is as defined above;

-   (f) subjecting the compound (6) to a retro-Diels-Alder reaction, to    form a compound of formula (7)

wherein Y is as defined above;

-   (g) treating the compound (7) with an oxidizing agent, to form a    compound of formula (8)

wherein Y is as defined above;

-   (h) reducing the compound (8) with a reducing agent, to form a    compound of formula (9)

wherein Y is as defined above;

-   (i) subjecting the compound (9) to a Mitsunobu reaction, to form a    compound of formula (10)

wherein Y is as defined above, followed by deprotection.

The process for the preparation of neplanocin A is illustrated below, inorder of steps (a) to (i).

Step (a)

Depending on the halogenating agent and the solvent used, the reactionmay be carried out at a temperature of about −20 to 20° C., preferablyabout 0° C., for about 1 to 10 hrs, preferably 2 hrs. As a reactionsolvent may be used a halogenated hydrocarbon solvent such asdichloromethane, chloroform and dichloroethane. The halogenating agentssuch as brominating, chlorinating and iodinating agents are well knownin the art of organic synthesis. Examples of such halogenating agentsinclude, but are not limited, to HBr, diphos-Br₂, N-bromosuccinimide(NBS), thionyl bromide, HCl, diphos-Cl₂, N-chlorosuccinimide (NCS) andthionyl chloride.

Step (b)

The agents for the-protection of hydroxyl groups (called “protectingagent” hereafter) may be selected from any agent known in the art oforganic synthesis for the protection of hydroxyl groups, for example,but not limited to halides including chlorides or bromides oftrimethylsilyl, triethylsilyl, t-butyldimethylsilyl,t-butyldiphenylsilyl, methoxymethyl, methoxyethoxymethyl, t-butyl,benzyl, triphenylmethyl, isopropyldimethylsilyl, tribenzylsilyl,triisopropylsilyl or the like.

Depending on the protecting agent and solvent used, the reaction may becarried out at a temperature of about −20 to 40° C., for about 10 to 20hrs. As a solvent may be used a base such as imidazole, benzimidazole,triethylamine, pyridine and hexamethylene disilazane. A base forfixation of free halogenated hydrogen may also be used as the solvent.Where the protecting agent is each kind of silyl chlorides andmethoxyethoxymethyl halides, the above-mentioned bases are used. Wherethe protecting agent is benzyl halides and methoxymethyl halides, sodiumhydride is used as the base. Where the hydroxyl group is protected witht-butyl group, the reaction is carried out with isobutene in thepresence of an acid type catalyst such as sulfuric acid.

Step (c)

The oxidizing agents used may be selected from any of a variety of theagents known in the art of synthetic organic chemistry, for example, butnot limited to, osmium tetraoxide, potassium permanganate, leadtetraacetate, ruthenium tetraoxide and selenium dioxide+hydrogenperoxide, with osmium tetraoxide being most preferred.

Depending on the oxidizing agent and solvent used, the reaction may becarried out at a temperature of about −20 to 40° C., for about 1 to 30hrs. As a reaction solvent may be used a polar solvent such as water andtetrahydrofuran (THF). Where the oxidizing agent is catalytically used,the reaction is carried out in the presence of an oxygen source such asmethylmorpholine N-oxide.

Step (d)

The ketalizing agents may be selected from acetals such as2,2-dimethoxypropane, 2,2-diethoxypropane or the like.

Depending on the ketalizing agent, solvent and catalyst used, thereaction may be carried out at a temperature of about −20 to 40° C.,preferably around room temperature, for about 15 to 30 hrs. The reactionsolvents which may be used are relatively low boiling point solvents(excluding alcohols) among conventional solvents, such as acetone,methyl ethyl ketone, hydrocarbons, halogenated hydrocarbons, diethylether, diisopropyl ether and THF. The catalysts which may be used in thereaction are acid type catalysts such as hydrochloric acid, ammoniumchloride, p-toluene-sulfonic acid, pyridinium p-toluenesulfonate,aluminum chloride and an acid type ion-exchange resin.

Step (e)

The dehalogenating agents used may be selected from any of a variety ofthe agents known in the art of synthetic organic chemistry, for example,but not limited to, active zinc dust, magnesium, sodium, palladium,sodium iodide and potassium iodide.

Depending on the dehalogenating agent and solvent used, the reaction maybe carried out under heat at reflux, for about 5 to 20 hrs. The reactionsolvents which may be used are alcohols such as methanol, ethanol,propanol and isopropanol, with methanol being preferable.

Step (f)

The retro-Diels-Alder reaction used here refers to thermal dissociationof Diels-Alder adducts, occurring most readily when one or bothfragments are particularly stable (see, Organic Name Reactions attachedto The Merck Index, 12th Edn.) The reaction may be carried out underheat at reflux in a high boiling point solvent, for about 20 to 60minutes. Such solvents are chemically stable, high boiling pointsolvents having a boiling point of 250 to 300° C. Diphenyl ether,α-chloronaphthalene, methyl α-naphthyl ether, ethyl α-naphthyl ether anddibenzyl ether are preferable.

Step (g)

The oxidizing agents may be selected from any of a variety of the agentsknown in the art of synthetic organic chemistry, for example, but notlimited to, chromic acid (VI), pyridinium dichromate, pyridiniumchlorochromate, chromium oxide (VI)—pyridine complex, manganese dioxide,dimethyl sulfoxide, hypohalorite and ruthenium tetraoxide.

Depending on the oxidizing agent and solvent used, the reaction may becarried out at a temperature of about 0 to 30° C., for about 1 to 10hrs. The reaction solvents which may be used are any solvent if it isliquid in the neighborhood of the reaction temperature and is stable tothe oxidizing agent. Halogenated hydrocarbons are preferable, such asdichloromethane, 1,2-dichloroethane and chloroform.

Step (h)

The reducing agents may be selected from any of a variety of the agentsknown in the art of synthetic organic chemistry, for example, but notlimited to, diisobutylaluminum hydride, lithium aluminum hydride,triisobutylaluminum, trialkoxy derivatives of lithium aluminumhydroxide, sodium bis(2-methoxyethoxy)aluminum hydride, sodiumborohydride, trimethoxy sodium borohydride, lithium borohydride,tri-sec-butyl lithium borohydride and tri-sec-butyl potassiumborohydride.

Depending on the reducing agent and solvent used, the reaction may becarried out at a temperature of about −78 to 0° C., for about 1 to 5hrs. The reaction solvents which may be used are any solvent if it isliquid at low temperature and is stable to the reducing agent. Toluene,benzene and THF are preferable.

Step (i)

The Mitsunobu reaction used here refers to condensation of alcohols andacidic components on treatment with dialkyl azodicarboxylates andtrialkyl- or triarylphosphines occurring primarily with inversion ofconfiguration via the proposed intermediary oxyphosphonium salts (see,Organic Name Reactions attached to The Merck Index, 12 Edn.)

Depending on the reactant and solvent used, the reaction may be carriedout at a temperature between 0° C. and room temperature, for about 4 to12 hrs. The reaction solvents which may be used are any solvent if it isgood solvent inert to the starting compound used in the Mitsunobureaction and the resulting compound, and is liquid in the neighborhoodof the reaction temperature. THF and 1,3-dioxane are preferable.

The deprotection in step (i) can be carried out in conventional manner.

The present invention also provides a process for preparing an opticallyactive compound of formula (1′)

which comprises subjecting a racemic compound of formula (11)

to a transesterification with an acylating agent in the presence of ahydrolase to optically resolve the racemic compound into an opticallyactive diester of formula (12)

wherein R₃ is an alkyl group of 1–19 carbons, and a monoester of formula(13)

wherein R₃ is as defined above, followed by alcoholysis.

The transesterification can be carried out under conventional conditionswith an acylating agent which has an acyl group of R₃COO(R₃ is an alkylgroup of 1–19 carbons) in the presence of a hydrolase. Examples of thealkyl groups of 1–19 carbons include, but are not limited to, methyl,ethyl, propyl, isopropyl, butyl, sec-butyl, tert-butyl, pentyl, heptyl,octyl, nonyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl,heptadecyl, octadecyl and nonadecyl.

PREFERRED EMBODIMENTS OF THE INVENTION

The processes of the present invention can be performed as discussedbelow. When the designated compounds show either one of enantiomers inthe optically active compounds, it is marked with the prime mark (′)except for the case of the compound (1′).

The compound of formula (11) in a racemic form which can be used as astarting material in the present processes may be prepared by reducingthe compound (16) prepared by Zwanenburg et al.'s method (Tetrahedron,1985, 41, 963). As shown in the following scheme A, the compound (16)may be prepared by epoxidizing the compound (14) with aqueous hydrogenperoxide followed by a Favorskii rearrangement. The Favorskiirearrangement refers to a base-catalyzed rearrangement of α-haloketonesor α,β-epoxyketones to acids or esters. The compound (14) is formed froma Diels-Alder reaction of cyclopentadiene and 1,4-benzoquinone which areeasily available. The compound (16) is reduced with diisobutylaluminumhydride (DIBAL), thus leading to the compound (11).

The resulting racemic compound (11) can be optically resolved into thecorresponding optically active diester (12) and monoester (13), by thetransesterification with the acylating agent in the presence of thehydrolase. The hydrolases which can be used herein, include, but are notlimited to, lipase, esterase, protease and lipoprotein lipase. Thosehydrolases may be any of animal, plant and fungus origins and may becommercially available immobilized products or dried extracts. Thoseoriginated from pseudomonas, candida and pancreatin are preferable. Theacylating agents which can be used in the present process include, butare not limited to, fatty acid anhydrides, fatty acid esters or thelike. More specifically, triglyceride, acetic anhydride, fatty acidtrichloroethyl esters, fatty acid isopropenyl esters and fatty acidvinyl esters can be used, and fatty acid vinyl esters are especiallypreferable. The reaction solvents which can be used include ethers,alkanes, benzene derivatives, halogenated hydrocarbon solvents, e.g.,acetonitrile, acetone, dimethylformamide (DMF), dimethyl sulfoxide(DMSO), diethyl ether, diisopropyl ether and t-butyl methyl ether.Diethyl ether, diisopropyl ether and t-butyl methyl ether arepreferable. The reaction temperature is in the range of −20° C. to 200°C., preferably 20° C. to 40° C. The reaction time is in the range of 1to 20 hrs., preferably 5 to 8 hrs. The treatment for purification afterreaction can use general separation method such as silica gel columnchromatography after the hydrolase is filtered off, by which eachcompound can be isolated and obtained.

As shown in the following scheme B, the resulting optically activediester (12′) and monoester (13′) can be subjected to the alcoholysiswith an alcohol e.g., methanol in the presence of a suitable base suchas potassium carbonate, thus leading to the optically active diol (1′).

The (+)-form of the resulting diol (1′) can lead to (−)-neplanocin A,and the (−)-form of the diol (1′) can lead to (+)-neplanocin A.

The process for preparing (−)-neplanocin A is discussed below, but(+)-neplanocin A which is its enantiomer can be prepared in a similarmanner, starting from the (−)-form of the diol (1′).

The (+)-form of the diol (1′) is reacted with a brominating agent suchas N-bromosuccinimide to afford(+)-9-bromo-2-hydroxymethyl-5,8-epoxytricyclo[5.2.1.0^(2,6)]dec-3-ene(2a′). It is preferable that the reaction solvent uses halogenatedhydrocarbon solvents such as dichloromethane. The reaction temperatureis in the range of −20° C. to 20° C., preferably about 0° C. Thereaction time is in the range of 1 to 10 hrs., preferably 2 hrs.

The above compound (2a′) and t-butyldimethylsilyl chloride are reactedfor 10–20 hrs in the presence of a suitable base such as imidazole toafford(+)-9-bromo-2-t-butyldimethylsilyloxymethyl-5,8-epoxytricyclo[5.2.1.0^(2,6)]dec-3-ene(3a′) wherein the primary hydroxyl group in the compound (2a′) isprotected with t-butyldimethylsilyl group.

The compound (3a′), because of taking a cage stereostructure, can betreated with a suitable oxidizing agent such as osmium tetraoxide, thusleading stereoselectively and regiospecifically to(+)-9-bromo-2-t-butyldimethylsilyloxymethyl-3,4-dihydroxy-5,8-epoxytricyclo[5.2.1.0^(2,6)]decane(4a′).

The reaction of two hydroxyl groups newly formed in said compound (4a′)with dimethoxypropane affords(+)-9-bromo-2-t-butyldimethylsilyloxymethyl-3,4-[(dimethyl-methylene)dioxy]-5,8-epoxytricyclo[5.2.1.0^(2,6)]decane(5a′).

The compound (5a′) is treated with active zinc powder to afford(+)-2-t-butyldimethylsilyloxymethyl-3,4-[(dimethylmethylene)dioxy]-5-hydroxy-tricyclo[5.2.1.0^(2,6)]dec-8-ene(6a′).

The compound (6a′) can be heated to reflux in diphenyl ether or can besubjected to a flush vacuum thermolysis to induce a retro-Diels-Alderreaction, thus leading to(−)-(1R,4R,5S)-3-(t-butyldimethylsilyloxymethyl)-4,5-[(dimethylmethylene)dioxy]-2-cyclopentene-1-ol(7a′).

The treatment of the hydroxyl group in the compound (7a′) with asuitable oxidizing agent such as pyridinium dichromate and pyridiniumchlorochromate affords(−)-(4R,5S)-3-(t-butyldimethylsilyloxymethyl)-4,5-[(dimethylmethylene)dioxy]-2-cyclopentene-1-one(8a′).

Reduction of the compound (8a′) with a reducing agent such as diisobutylaluminum hydride, lithium aluminum hydride or the like can leadstereospecifically to(+)-(1S,4R,5S)-3-(t-butyldimethylsilyloxymethyl)-4,5-[(dimethyl-methylene)dioxy]-2-cyclopentene-1-ol(9a′) wherein the hydroxyl group at the 1-position of the compound (7a′)is inversed.

Combining the compound (9a′) with adenine by a Mitsunobu reaction canlead to(−)-(1′R,4′R,5′S)-3′-(t-butyldimethylsilyloxymethyl)-4′,5′-[(dimethylmethylene)-dioxy]-2′-cyclopentene-1′-yl]adenine(10a′). Finally, the compound (10a′) is deprotected using a purificationmethod with an ion-exchange resin to afford (−)-neplanocin A.

The invention is further illustrated by the following Examples. Theseexamples are presented to exemplify the invention and are not to beconstrued as limiting the invention's scope.

REFERENTIAL EXAMPLE 1

A solution of tricyclo[6.2.1.0^(2,7)]undeca-4,9-diene-3,6-dione (14)(26.13 g, 150 mmol) in acetone (100 ml) was cooled to 0° C. on anice-bath. To the solution was added saturated aqueous NaHCO₃ (33 ml). Tothe mixture was added dropwise 34.5% aqueous hydrogen peroxide (142 ml)while keeping at 0° C. After the addition, the reaction mixture wasstirred at 0° C. for 1 hr and then water (100 ml) was added. From themixture solution, the product was extracted with diethyl ether (total700 ml). The extract was washed with saturated aqueous NaCl and driedover magnesium sulfate, and the solvent was distilled off under reducedpressure to afford as the residue4,5-epoxy-tricyclo[6.2.1.0^(2,7)]undec-9-ene-3,6-dione (15) (28.06 g,148 mmol, 98.35% yield) in light yellowish white crystals.

REFERENTIAL EXAMPLE 2

A suspension of 4,5-epoxy-tricyclo[6.2.1.0^(2,7)]undec-9-ene-3,6-dione(15) (9.28 g, 48.8 mmol) in ethanol (50 ml) was heated to 45° C. To thesuspension was added dropwise a 5 M-ethanol solution of sodium hydroxide(18 ml) over a period of 30 minutes. From the reaction mixture, ethanolwas distilled off under reduced pressure. The residue was dissolved withdiethyl ether (300 ml), washed with saturated aqueous NaCl and driedover magnesium sulfate, and diethyl ether was distilled off underreduced pressure to afford as the residue5-oxo-tricyclo[5.2.1.0^(2,6)]deca-3,8-diene-2-carboxylate (16) (6.58 g,30.1 mmol, 61.78% yield) in dark brown liquid.

EXAMPLE 1

A solution of ethyl5-oxo-tricyclo[5.2.1.0^(2,6)]deca-3,8-diene-2-carboxylate (16) (1.84 g,8.43 mmol) in toluene (30 ml) was cooled to −78° C. under an argonatmosphere and stirred. To the reaction solution was added dropwise a1.5 M-toluene solution of diisobutylaluminum hydride (DIBAL) (19.7 ml,29.5 mmol) over a 25 minute period. The reaction mixture was stirred for3 hrs while keeping at −78° C. and aqueous ammonia was added whilecooling. The precipitated solid was filtered off through a glass funnel.The filtrate was concentrated under reduced pressure to afford 2.08 g ofthe residue (white solid) which was then subjected to silica gel columnchromatography (eluting solvent: n-hexane/ethyl acetate=1/1) to afford2-hydroxymethyl-5-hydroxy-tricyclo[5.2.1.0^(2,6)]deca-3,8-diene (11)(0.98 g, 5.5 mmol, 65% yield), with the following data:

IR (neat): ν=3270 cm⁻¹ ¹H NMR (CDCl₃): δ =1.60 (1H, d, J=8.8 Hz), 1.68(1H, d, J=8.8 Hz), 2.70 (2H, m), 2.96 (1H, s), 3.67 (1H, d, J=10.6 Hz),3.84 (1H, d, J=10.6 Hz), 4.76 (1H, s), 5.53 (1H, dd, J=5.5, 1.8 Hz).

EXAMPLE 2

A suspension of2-hydroxymethyl-5-hydroxy-tricyclo[5.2.1.0^(2,6)]deca-3,8-diene (11)(980 mg, 5.5 mmol) and vinyl acetate (758 mg, 8.8 mmol) in t-butylmethyl ether (3 ml) was stirred at room temperature. To the reactionsolution was added lipase (1 g, immobilized lipase originated frompseudomonas, manufactured by Toyobo Co., Ltd.) and the mixture wasstirred at room temperature for 8 hrs. Lipase was filtered off and thefiltrate was concentrated under reduced pressure to afford a yellowresidue. The residue was subjected to silica gel column chromatography(eluting solvent: n-hexane/ethyl acetate=3/1) to afford the diacetate(12′) (590 mg, 2.25 mmol) and the monoacetate (13′) (495 mg, 2.25 mmol),respectively, with the following data:

For (−)-diacetate (12′)

IR (neat): ν=2967, 1734 cm⁻¹ ¹H NMR (CDCl₃): δ=1.52 (1H, d, J=8.8 Hz),1.60 (1H, d, J=8.8 Hz), 1.99 (3H, s), 2.01 (3H, s), 2.69 (1H, br s),2.74 (1H, br s), 4.07 (1H, d, J=10.7 Hz), 4.34 (1H, d, J=10.7 Hz), 5.50(2H, m), 5.95 (2H, m) MS: m/z=262 (M+). Anal. Calcd. for C15H18O4 (M+):m/z=262.1205. Found: m/z=262.1203.

For (+)-monoacetate (13′)

IR (neat): ν=3440, 2962, 1730 cm⁻¹ ¹H NMR (CDCl₃): δ=1.60 (1H, d, J=8.8Hz), 1.68 (1H, d, J=8.8 Hz), 2.05 (3H, s), 2.64 (1H, m), 2.78 (1H, brs), 2.94 (1H, br s), 4,12 (1H, d. J=10.7 Hz), 4.36 (1H, d, J=10.7 Hz),4.76 (1H, d, J=10.2 Hz), 5.54 (1H, d, J=1.4 Hz), 5.59 (1H, d, J=1.4 Hz),5.92 (1H, m), 6.16 (1H, m) MS: m/z=220 (M+). Calcd. for Cl3Hl6O3 (M+):m/z=220.1099. Found: m/z=220.1104.

To a solution of the resultant diacetate (12′) (590 mg) in methanol (20ml) was added potassium carbonate (691 mg, 5.0 mmol) and the mixture wasstirred at room temperature for 8 hrs. The reaction product wasextracted with ethyl acetate (40 ml). The organic layer was washed withsaturated aqueous NaCl, dried over magnesium sulfate and concentratedunder reduced pressure to afford(−)-2-hydroxymethyl-5-hydroxy-tricyclo[5.2.1.0^(2,6)]deca-3,8-diene (330mg, 1.85 mmol) having the following specific rotation:

[α]_(D) ²⁶−168.11° (cl. 03, EtOH).

According to a conventional method, further, this compound was led tothe dibenzoate which was analyzed with an optical resolution column(Chiral Cell OD manufactured by Daicel Co., Ltd.,5%-isopropanol-n-hexane solution), by which it was found 92% ee.

For the monoacetate (13′), similar procedure was carried out except forusing 373 mg(2.7 mmol) of potassium carbonate, thereby affording(+)-2-hydroxymethyl-5-hydroxy-tricyclo[5.2.1.0^(2,6)]deca-3,8-diene (367mg, 2.06 mmol) having the following specific rotation and melting point:

[α]_(D) ³⁰+154.86° (cl. 01, EtOH), m.p. 116–119° C.

According to a conventional method, further, this compound was led tothe dibenzoate which was analyzed with an optical resolution column(Chiral Cell OD manufactured by Daicel Co., Ltd.,5%-isopropanol-n-hexane solution), by which it was found >99% ee.

EXAMPLE 3

A solution of(+)-2-hydroxymethyl-5-hydroxy-tricyclo[5.2.1.0^(2,6)]deca-3,8-diene((+)-form of Compound (1′)) (287 mg, 1.6 mmol) obtained in Example 2 indichloromethane (30 ml) was cooled to 0° C. and stirred. To the solutionwas added N-bromosuccinimide (322 mg, 1.8 mmol) and the mixture wasstirred for 2 hrs while keeping at 0° C. The reaction solution wasconcentrated under reduced pressure and the resulting residue wassubjected to silica gel column chromatography (eluting solvent:n-hexane/ethyl acetate=2/1) to afford(+)-9-bromo-2-hydroxymethyl-5,8-epoxytricyclo-[5.2.1.0^(2,6)]dec-3-ene(2a′) (414 mg, 1.6 mmol, 99.6% yield), with the following data:

[α]_(D) ²⁹+153.15° (c0.302, CHCl₃) IR (neat): ν=3409, 2972 cm⁻¹ ¹H NMR(CDCl₃): δ=1.73 (1H, br), 2.17–2.38 (1H, m), 3.48 (2H, d), 4.08 (1H, d),4.56–4.69 (3H, m), 5.70 (1H, m), 6.0 (1H, m) MS: m/z=256 (M+). Calcd.for C11Hl3BrO2 (M+): m/z=256.0098. Found: m/z=256.0112.

EXAMPLE 4

To a solution of(+)-9-bromo-2-hydroxymethyl-5,8-epoxytricyclo[5.2.1.0^(2,6)]dec-3-ene(2a′) (319 mg, 1.24 mmol) and imidazole (126.5 mg, 1.86 mmol) in DMF (30ml) was added t-butyldimethylsilyl chloride (242 mg, 1.6 mmol), and themixture was stirred overnight at room temperature and diluted withn-hexane (80 ml). The organic layer was washed with saturated aqueousNaCl, dried over magnesium sulfate and concentrated under reducedpressure to obtain the residue. Silica gel column chromatography(eluting solvent: n-hexane/diethyl ether=2/1) of the residue afforded(+)-9-bromo-2-(t-butyldimethylsilyloxymethyl)-5,8-epoxytricyclo[5.2.1.0^(2,6)]dec-3-ene (3a′) (447 mg,1.20 mmol, 97% yield), with the following data:

[α]_(D) ²⁸+114.06° (c0.161, CHCl₃) IR (neat): ν=2954, 2856, 1471, 1377cm⁻¹ ¹H NMR (CDCl₃): δ=0.013 (6H, s), 0.86 (9H, s), 2.16–2.38 (2H, m),2.39–2.65 (3H, m), 3.40 (1H, d, J=10.0 Hz), 3.77 (1H, d, J=10.0 Hz),4.13 (1H, d, J=2.5 Hz), 4.61 (2H, m), 5.77 (1H, d, J=5.7 Hz), 5.95 (1H,dd, J=5.7, 2.5 Hz) MS: m/z=355 (M+ −Me). Calcd. for C16H24BrO2Si (M+−Me): m/z=355.0763. Found: m/z=355.0729.

EXAMPLE 5

A solution of(+)-9-bromo-2-(t-butyldimethyl-silyloxymethyl)-5,8-epoxytricyclo[5.2.1.0^(2,6)]dec-3-ene (3a′) (283 mg, 0.762 mmol) in a mixed solvent of THF (15 ml)and water (5 ml) was cooled to 0° C. and stirred. To the solution wereadded 4-methylmorpholine N-oxide (155 mg, 1.14 mmol) and a 0.197 M-THFsolution of osmium tetraoxide (1.5 ml, 0.3 mmol). Subsequently, themixture was allowed to warm up to room temperature and stirredovernight. A 10% aqueous solution of sodium sulfite (15 ml) was addedand the mixture was filtered through Celite. The filtered product waswashed thoroughly with water, THF and diethyl ether. The combinedwashings and filtrate were diluted with diethyl ether (80 ml). Theorganic layer was washed with saturated aqueous NaHCO₃ and saturatedaqueous NaCl, respectively, and dried over magnesium sulfate.Subsequently, the solvent was distilled off under reduced pressure toobtain the residue. Silica gel column chromatography (eluting solvent:n-hexane/diethyl ether=2/1) of the residue afforded(+)-9-bromo-2-(t-butyldimethylsilyloxymethyl)-3,4-dihydroxy-5,8-epoxytricyclo[5.2.1.0^(2,6)]decane(4a′) (246 mg, 0.607 mmol, 80% yield), with the following data:

[α]_(D) ²⁸+57.15° (c0.26, CHCl₃) ¹H NMR (CDCl₃): δ=0,099 (6H, s), 0.89(9H, s), 1.65 (1H, brs), 1.95 (1H, d, J=10.9 Hz), 2.16–2.38 (2H, m),2.37 (2H, m), 2.62 (1H, t, J=4.4 Hz), 2.77 (1H, m), 3.05 (1H, d, J=5.2Hz), 3.51 (1H, d, J=5.5 Hz), 3.60 (1H, d, J=10.2 Hz), 3.81 (1H, d, J=9.9Hz), 4.15 (2H, m), 4.39 (1H, t, J=4.9 Hz), 4.53 (1H, d, J=4.9 Hz) MS:m/z=389 (M+ −Me). Calcd. for C16H26BrO4Si (M+ −Me): m/z=389.0318. Found:m/z=389.0397.

EXAMPLE 6

To a solution of(+)-9-bromo-2-(t-butyldimethyl-silyloxymethyl)-3,4-dihydroxy-5,8-epoxytricyclo[5.2.1.0^(2,6)]-decane(4a′) (186 mg, 0.459 mmol) in acetone (30 ml) were addeddimethoxypropane (72 mg, 0.69 mmol) and pyridinium p-toluenesulfonate(15 mg) and the mixture was stirred overnight at room temperature. Tothe reaction solution was added diethyl ether (50 ml) and the mixturewas washed with saturated aqueous NaHCO₃ and saturated aqueous NaCl.This solution was dried over magnesium sulfate and concentrated underreduced pressure to obtain the residue. Silica gel column chromatography(eluting solvent: n-hexane/ethyl acetate=3/1) of the residue afforded(+)-9-bromo-2-(t-butyldimethylsilyloxymethyl)-3,4-[(dimethylmethylene)dioxy]-5,8-epoxytricyclo[5.2.1.0^(2,6)]decane(5a′) (205 mg, 0.46 mmol), 100% yield), with the following data:

[α]_(D) ²⁹+73.15° (c0.12, CHCl₃) IR (neat): ν=2928, 2855, 1471, 1380cm⁻¹ ¹H NMR (CDCl₃): δ=0.023 (6H, s), 0.86 (9H, s), 1.24 (3H, s), 1.41(3H, s), 2.02–2.19 (2H, m), 2.36 (1H, m), 2.69 (1H, m), 3.47 (1H, d,J=9.9 Hz), 3.63 (1H, d, J=2.5 Hz), 3.98 (1H, d, J=9.6 Hz), 4.37 (1H, d,J=5.7 Hz), 4.54 (1H, m), 4.60 (1H, d, J=5.5 Hz) MS: m/z=429 (M+ −Me).Calcd. for C19H30BrO4Si (M+ −Me): m/z=429.1131. Found: m/z=429.1090.

EXAMPLE 7

To a solution of(+)-9-bromo-2-(t-butyldimethyl-silyloxymethyl)-3,4-[(dimethylmethylene)dioxy]-5,8-epoxy-tricyclo[5.2.1.0^(2,6)]decane(5a′) (205 mg, 0.46 mmol) in methanol (30 ml) were added active zincpowder (182 mg, 2.76 mmol) and acetic acid (0.1 ml), and the mixture washeated to reflux for 10 hrs. The reaction solution was filtered throughCelite and the filtered mass was washed with methanol. The combinedwashings and filtrate were diluted with diethyl ether (80 ml) and washedwith saturated aqueous NaHCO₃ and saturated aqueous NaCl. This solutionwas dried over magnesium sulfate and concentrated under reduced pressureto afford(+)-2-(t-butyldimethylsilyloxymethyl)-3,4-[(dimethylmethylene)dioxy]-5-hydroxy-tricyclo[5.2.1.0^(2,6)]-dec-8-ene(6a′) (160 mg, 0.44 mmol, 95% yield) in colorless powdery crystals, withthe following data:

[α]_(D) ³⁰+147.0° (c0.30, CHCl₃) IR (Nujol): ν=3313, 2924, 2854, 1462,1376 cm⁻¹ ¹H NMR (CDCl₃): δ=0.023 (6H, s), 0.87 (9H, s), 1.18 (3H, s),1.41 (4H, m), 1.58 (1H, m), 1.78 (1H, brs), 2.40 (1H, m), 2.86 (1H, s),3.05 (1H, s), 3.52 (1H, d, J=9.6 Hz), 3.99 (1H, d, J=4.9 Hz), 4.07–4.12(3H, m), 6.20 (1H, m), 6.32 (1H, m) MS: m/z=366 (M+). Calcd. forC20H34O4Si (M+): m/z=366.2226. Found: m/z=366.2242.

EXAMPLE 8

A solution of(+)-2-(t-butyldimethyl-silyloxymethyl)-3,4-[(dimethylmethylene)dioxy]-5-hydroxy-tricyclo[5.2.1.0^(2,6)]dec-8-ene(6a′) (280 mg, 0.76 mmol) in diphenyl ether (5 ml) was heated to refluxfor 30 minutes. The reaction solution was subjected to silica gel columnchromatography (eluting solvent: n-hexane/diethyl ether=1/1) to afford(−)-(1R,4R,5S)-3-(t-butyldimethylsilyloxymethyl)-4,5-[(dimethylmethylene)dioxy]-2-cyclopenten-1-ol(7a′) (225 mg, 0.749 mmol, 98.7% yield), with the following data:

[α]_(D) ³²−21.53° (c0.54, CHCl₃) IR (neat): ν=3405, 2930, 2857, 1372cm⁻¹ ¹H NMR (CDCl₃): δ=0.086 (6H, s), 0.92 (9H, s), 1.36 (6H, d, J=11.2Hz), 1.98 (1H, d, J=6.3 Hz), 4.33 (2H, m), 4.55 (1H, d, J=5.8 Hz), 4.72(1H, m), 5.13 (1H, d, J=5.8 Hz), 5.75 (1H, d, J=1.1 Hz) MS: m/z=285 (M+−Me). Calcd. for C14H25O4Si (M+ −Me): m/z=285.1557. Found: m/z=285.1502.

EXAMPLE 9

To a solution of(−)-(1R,4R,5S)-3-(t-butyldimethylsilyloxymethyl)-4,5-[(dimethylmethylene)dioxy]-2-cyclopenten-1-ol(7a′) (225 mg, 0.749 mmol) in dichloromethane (50 ml) was addedpyridinium dichromate (425 mg, 1.13 mmol) and the mixture was stirred atroom temperature for 2 hrs. The reaction solution was filtered throughCelite and the filtrate was concentrated under reduced pressure toobtain the residue. Silica gel column chromatography (eluting solvent:n-hexane/diethyl ether=1/1) of the residue afforded(−)-(4R,5S)-3-(t-butyldimethyl-silyloxymethyl)-4,5-[(dimethylmethylene)dioxy]-2-cyclopenten-1-one(8a′) (186 mg, 0.623 mmol, 83% yield), with the following data:

[α]²⁹−10.67° (c0.85, CHCl₃). IR (neat): ν=2955, 2931, 2857, 1725 cm⁻¹ ¹HNMR (CDCl₃): δ=0.076 (6H, s), 0.89. (9H, s), 1.38 (6H, s), 4.41–4.68(3H, m), 5.03 (1H, d, J=5.8 Hz), 6.14 (1H, t, J=1.9 Hz) MS: m/z=283 (M+−Me). Calcd. for C14H23O4Si (M+ −Me): m/z=283.14. Found: m/z=283.1377.

EXAMPLE 10

A solution of(−)-(4R,5S)-3-(t-butyldimethyl-silyloxymethyl)-4,5-[(dimethylmethylene)dioxy]-2-cyclopenten-1-one(8a′) (186 mg, 0.623 mmol) in toluene (10 ml) was cooled to −78° C. Tothe solution was added dropwise a 1.5 M-toluene solution ofdiisobutylaluminum hydride (0.62 ml, 0.93 mmol), and the mixture wasstirred at −78° C. for 2 hrs. The reaction solution diluted withmethanol and water, respectively was extracted with chloroform. Theorganic layer was washed with saturated aqueous NaCl, dried overmagnesium sulfate and concentrated under reduced pressure. The residuewas subjected to silica gel column chromatography (eluting solvent:n-hexane/diethyl ether=1/1) to afford(+)-(1S,4R,5S)-3-(t-butyldimethyl-silyloxymethyl)-4,5-[(dimethylmethylene)dioxy]-2-cyclopenten-1-ol(9a′) (186 mg, 0.62 mmol, 100% yield), with the following data:

[α]_(D) ²⁹+22.53° (c0.63, CHCl₃). IR (neat): ν=2954, 2930, 2857, 1372cm⁻¹ ¹H NMR (CDCl₃): δ=0.05 (6H, s), 0.89 (9H, s), 1.38 (6H, d, J=8.8Hz), 2.65 (1H, d, J=10.2 Hz), 4.17–4.35 (2H, m), 4.52 (1H, m), 4.74 (1H,m), 4.87 (1H, m), 5.71 (1H, t, J=0.8 Hz) MS: m/z=285 (M+ −Me). Calcd.for C14H25O4Si (M+ −Me): m/z=285.1557. Found: m/z=285.1529.

EXAMPLE 11

A solution of(+)-(1S,4R,5S)-3-(t-butyldimethyl-silyloxymethyl)-4,5-[(dimethylmethylene)dioxy]-2-cyclopenten-1-ol(9a′) (145 mg, 0.48 mmol), adenine (272 mg, 1.92 mmol) andtriphenylphosphine (529 mg, 2.02 mmol) in THF (90 ml) was cooled to 0°C. To the cooled solution was added dropwise diisopropylazodicarboxylate (408 mg, 2.02 mmol), and the mixture was allowed towarm up to room temperature and stirred for 8 hrs. The reaction solutionwas concentrated under reduced pressure and the resulting residue wassubjected to silica gel column chromatography (eluting solvent:chloroform/ethanol=10/1) to afford(−)-[(1′R,4′R,5′S)-3′-(t-butyldimethylsilyloxymethyl)-4′,5′-[(dimethylmethylene)dioxy]-2′-cyclopentene1′-yl]adenine(10a′) (148 mg, 0.40 mmol, 84% yield), with the following data:

[α]_(D) ²⁹−31.57° (c0.29, CHCl₃) IR (neat): ν=3322, 3171, 2954, 2931,2857, 1645, 1597 cm⁻¹ ¹H NMR (CDCl₃): δ=0.10 (6H, s), 0.92 (9H, s), 1.35(3H, s), 1.48 (3H, s), 4.43 (2H, m), 4.70 (1H, d, J=5.8 Hz), 5.31 (1H,d, J=5.2 Hz), 5.59(1H, m), 5.75 (1H, s), 5.78 (2H, brs), 7.68 (1H, s),8.39 (1H, s) MS: m/z=412 (M+ −Me). Calcd. for C19H28N5O3Si (M+ −Me):m/z=402.1996. Found: m/z=402.1935.

EXAMPLE 12

A solution of(−)-[(1′R,4′R,5′S)-3′-(t-butyldimethylsilyloxymethyl)-4′,5′-[(dimethylmethylene)-dioxy]-2′-cyclopentene-1′-yl]adenine(10a′) (138 mg, 0.33 mmol) in a mixed solvent of methanol (20 ml) and1N-hydrochloric acid (20 ml) was stirred at room temperature for 3 hrs.The reaction solution was concentrated under reduced pressure, and theresulting residue was dissolved in water (1 ml) and passed through anion exchange resin column (Dowex 50, H⁺ form). This column was washed bypassing pure water therethrough and then eluted with 5% aqueous ammonia.The resulting eluate was concentrated under reduced pressure to obtainwhite crystals. Recrystallization from methanol afforded (−)-NeplanocinA (78 mg, 0.30 mmol, 90% yield), with the following physical values:

[α]_(D) ²⁹−31.57° (c0.29, CHCl₃), m.p. 217–219° C.

These values agreed closely with those given in the literature.

INDUSTRIAL APPLICABILITY

According to the present invention, there can be prepared opticallyactive 2-hydroxymethyl-5-hydroxy-tricyclo[5.2.1.0^(2,6)]deca-3,8-diene(1′) which is a chiral element useful in the organic synthesis. Thepresent invention can also provide the process for efficiently preparingneplanocin A in 10 steps and in 45% overall yield, starting from thecompound (1′).

1. A compound of formula (6)

wherein Y is a protecting group.
 2. A compound of claim 1 wherein Y ist-butyldimethylsilyl.